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人和豚鼠气道中功能性肾上腺素能受体的分化

Differentiation of functional adrenoceptors in human and guinea pig airways.

作者信息

Zaagsma J, van der Heijden P J, van der Schaar M W, Bank C M

出版信息

Eur J Respir Dis Suppl. 1984;135:16-33.

PMID:6203772
Abstract

The nature of the beta-adrenoceptor population(s) mediating direct smooth muscle relaxation, inhibition of antigen-induced histamine release and inhibition of antigen-induced (leukotriene-mediated) smooth muscle contraction of human and guinea pig central and peripheral airways was investigated. Preferential blockade by beta 1- and beta 2-selective antagonists of the relaxation induced by beta 1- and beta 2-selective agonists, respectively, revealed the guinea pig tracheal smooth muscle relaxation to be mediated by both beta 1- and beta 2-adrenoceptors. Using a highly beta 2-selective antagonist, the NE-induced relaxation was split up biphasically into a beta 1- and a beta 2-component. In contrast, no such differential blockade was observed with the relaxation of the guinea pig lung parenchyma strip, neither with the human tracheal, main bronchus and respiratory bronchiolus smooth muscle, which are all mediated by homogeneous beta 2-adrenoceptor populations. Only in the guinea pig trachea did neuronal and extraneuronal uptake inhibitors produce pronounced left shifts of the NE- and ISO-induced relaxation curves, respectively, suggesting a causal relationship between noradrenergic innervation and the presence of the beta 1-adrenoceptor subpopulation in the airways. Using the same techniques, it was established that inhibition of antigen-induced histamine release from guinea pig lung and tracheal mast cells is mediated by homogeneous beta 2-adrenoceptor populations as well. In contrast to catecholamines, non-catecholamine beta-agonists such as fenoterol, clenbuterol and zinterol had a substantially higher apparent affinity for the inhibition of the anaphylactic (leukotriene-mediated) guinea pig tracheal contraction than for the inhibition of histamine release; the same was true for lung tissue, though the difference was less pronounced. With some non-catecholamine beta-agonists considerable selectivity both in central and peripheral airway preparations was observed for the inhibition of anaphylactic contraction as compared with smooth muscle relaxation.

摘要

研究了介导人及豚鼠中枢和外周气道平滑肌直接舒张、抑制抗原诱导的组胺释放以及抑制抗原诱导的(白三烯介导的)平滑肌收缩的β-肾上腺素能受体群体的性质。β1-和β2-选择性拮抗剂分别优先阻断β1-和β2-选择性激动剂诱导的舒张,表明豚鼠气管平滑肌舒张由β1-和β2-肾上腺素能受体介导。使用高度β2-选择性拮抗剂,去甲肾上腺素(NE)诱导的舒张被双相分离为β1-和β2-成分。相比之下,豚鼠肺实质条带的舒张以及人气管、主支气管和呼吸细支气管平滑肌的舒张均未观察到这种差异阻断,这些均由均一的β2-肾上腺素能受体群体介导。仅在豚鼠气管中,神经元和非神经元摄取抑制剂分别使NE和异丙肾上腺素(ISO)诱导的舒张曲线明显左移,提示去甲肾上腺素能神经支配与气道中β1-肾上腺素能受体亚群的存在之间存在因果关系。使用相同技术还确定,抑制豚鼠肺和气管肥大细胞抗原诱导的组胺释放也由均一的β2-肾上腺素能受体群体介导。与儿茶酚胺不同,非儿茶酚胺β-激动剂如非诺特罗、克仑特罗和齐帕特罗对抑制过敏性(白三烯介导的)豚鼠气管收缩的表观亲和力明显高于抑制组胺释放;肺组织也是如此,尽管差异不太明显。对于一些非儿茶酚胺β-激动剂,在中枢和外周气道制剂中,与平滑肌舒张相比,观察到对过敏性收缩的抑制具有相当大的选择性。

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